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Pressure effect on the microphase separation of diblock copolymer melts studied by dynamic density functional theory based on equation of state

机译:基于状态方程的动态密度泛函理论研究二嵌段共聚物熔体微相分离的压力效应

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Pressure effect on the microphase separation of diblock copolymer melts was investigated by dynamic density functional theory based on the equation of state (EOS-based DDFT). The results show the corresponding counterparts in the experiment. With the increase of pressure, all of the phase regions corresponding to the different ordered morphologies become narrower. However, the pressure dependence of the order-disorder transition temperature (ToDT) lies on the symmetry of the diblock copolymer. In the very non-symmetrical case with f being small, Tour decreases with the increase of pressure, while in the symmetrical case when f=0.5, ToDT increases with increasing pressure. Moreover, the increase in the total bead number of system at the ODT is found to be in good accordance with the experimental results, specifically, there is an increase in the volume accompanying with the transition from the ordered to disordered state. Contrary to the temperature, the pressure does not influence the starting time and the duration of microphase separation.
机译:基于状态方程(基于EOS的DDFT),通过动态密度泛函理论研究了压力对二嵌段共聚物熔体微相分离的影响。结果显示了实验中相应的对应项。随着压力的增加,对应于不同有序形态的所有相区域变窄。但是,有序-无序转变温度(ToDT)的压力依赖性取决于二嵌段共聚物的对称性。在非常小的非对称情况下,f很小,Tour随着压力的增加而降低,而在对称情况下,当f = 0.5时,ToDT随着压力的增加而增加。此外,发现ODT处系统的总珠数的增加与实验结果很好地吻合,具体而言,伴随从有序状态到无序状态的转变,存在体积的增加。与温度相反,压力不影响微相分离的开始时间和持续时间。

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